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- NP788099.RAG_BL3kdCAMh__TxbKFU4J8TwLJfVqMMkMFhKh93fzgU130_assertion type Assertion NP788099.RAG_BL3kdCAMh__TxbKFU4J8TwLJfVqMMkMFhKh93fzgU130_head.
- NP788099.RAG_BL3kdCAMh__TxbKFU4J8TwLJfVqMMkMFhKh93fzgU130_assertion wasGeneratedBy ECO_0000203 NP788099.RAG_BL3kdCAMh__TxbKFU4J8TwLJfVqMMkMFhKh93fzgU130_provenance.
- NP788099.RAG_BL3kdCAMh__TxbKFU4J8TwLJfVqMMkMFhKh93fzgU130_assertion wasDerivedFrom befree-2016 NP788099.RAG_BL3kdCAMh__TxbKFU4J8TwLJfVqMMkMFhKh93fzgU130_provenance.
- NP788099.RAG_BL3kdCAMh__TxbKFU4J8TwLJfVqMMkMFhKh93fzgU130_assertion SIO_000772 20085575 NP788099.RAG_BL3kdCAMh__TxbKFU4J8TwLJfVqMMkMFhKh93fzgU130_provenance.
- NP788099.RAG_BL3kdCAMh__TxbKFU4J8TwLJfVqMMkMFhKh93fzgU130_assertion evidence source_evidence_literature NP788099.RAG_BL3kdCAMh__TxbKFU4J8TwLJfVqMMkMFhKh93fzgU130_provenance.
- NP788099.RAG_BL3kdCAMh__TxbKFU4J8TwLJfVqMMkMFhKh93fzgU130_assertion description "[The most frequent cytogenetic abnormalities were ETV6/RUNX1 fusion (16%) and trisomy 8 (14.6%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP788099.RAG_BL3kdCAMh__TxbKFU4J8TwLJfVqMMkMFhKh93fzgU130_provenance.